Mutation

Primary Site >> Stomach Cancer

Gene >> MAGI1

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000402939
Start	65391193:65391193(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs770193154
CDS Mutation	c.2365C>A
AA Mutation	p.Pro789Thr(p.P789T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000402939
Start	65356545:65356545(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs760749180
CDS Mutation	c.4222G>A
AA Mutation	p.Glu1408Lys(p.E1408K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000402939
Start	65442795:65442795(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs761124349
CDS Mutation	c.1133T>C
AA Mutation	p.Val378Ala(p.V378A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000402939
Start	65478606:65478606(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.743A>G
AA Mutation	p.Asn248Ser(p.N248S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000402939
Start	65356937:65356937(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs779070587
CDS Mutation	c.3830A>G
AA Mutation	p.Asn1277Ser(p.N1277S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000402939
Start	65430791:65430791(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs756694536
CDS Mutation	c.1454C>T
AA Mutation	p.Thr485Met(p.T485M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000402939
Start	65470439:65470439(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.803T>C
AA Mutation	p.Leu268Ser(p.L268S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000402939
Start	65430819:65430819(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs779881861
CDS Mutation	c.1426C>T
AA Mutation	p.Arg476Trp(p.R476W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000402939
Start	65356767:65356767(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs773042890
CDS Mutation	c.4000G>A
AA Mutation	p.Asp1334Asn(p.D1334N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000402939
Start	65356872:65356872(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3895C>T
AA Mutation	p.Arg1299Trp(p.R1299W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000402939
Start	65429584:65429584(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2103A>C
AA Mutation	p.Gln701His(p.Q701H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000402939
Start	66038292:66038292(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.17A>T
AA Mutation	p.Gln6Leu(p.Q6L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000402939
Start	65429901:65429901(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1786A>C
AA Mutation	p.Ser596Arg(p.S596R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000402939
Start	66038005:66038005(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.304G>T
AA Mutation	p.Val102Phe(p.V102F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	15
Mutation Consequence	missense_variant
Transcription ID	ENST00000402939
Start	65356706:65356706(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.4061G>T
AA Mutation	p.Arg1354Met(p.R1354M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	16
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000402939
Start	65375945:65375945(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2996G>T
AA Mutation	p.Gly999Val(p.G999V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	17
Mutation Consequence	missense_variant
Transcription ID	ENST00000402939
Start	65356806:65356806(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3961C>T
AA Mutation	p.Arg1321Trp(p.R1321W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	18
Mutation Consequence	missense_variant
Transcription ID	ENST00000402939
Start	65429841:65429841(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs151058544
CDS Mutation	c.1846G>A
AA Mutation	p.Val616Met(p.V616M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	19
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000402939
Start	65356459:65356459(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.4308G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	20
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000402939
Start	65356834:65356834(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3933C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	21
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000402939
Start	65357122:65357122(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3645C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	22
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000402939
Start	65381980:65381980(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2598G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	23
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000402939
Start	65356546:65356546(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.4221delC
AA Mutation	p.Glu1408SerfsTer27(p.E1408Sfs*27)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	24
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000402939
Start	65429959:65429960(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.1727dupT
AA Mutation	p.Leu576PhefsTer3(p.L576Ffs*3)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

ID	25
Mutation Consequence	splice_acceptor_variant
Transcription ID	ENST00000402939
Start	65493632:65493632(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.431-1G>T
Mutation Classification	Splice_Site
Feature Type	Transcript